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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Carbamic acid, (3-aminocyclohexyl)-, 1,1-dimethylethyl ester

NC1CCCC(C1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Carbamic acid, (3-aminocyclohexyl)-, 1,1-dimethylethyl ester
CAS Number: 347186-01-0
Product Number: AG0039SV(AGN-PC-03IKUH)
Synonyms:
MDL No:
Molecular Formula: C11H22N2O2
Molecular Weight: 214.3046

Identification/Properties

Computed Properties
Molecular Weight:
214.309g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
214.168g/mol
Monoisotopic Mass:
214.168g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
223
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (3-aminocyclohexyl)carbamate, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure, featuring a tert-butyl group and a cyclohexyl ring, offers a range of synthetic possibilities in organic chemistry.One of the key applications of $name$ is its use as a protecting group for amines. By selectively masking the amino group with the carbamate functionality, $name$ enables the manipulation of other functional groups without interfering with the amine moiety. This protection strategy is especially valuable in multi-step synthesis, where the presence of reactive amine groups could lead to unwanted side reactions.In addition to its role as a protecting group, $name$ can also serve as a precursor for the synthesis of various nitrogen-containing compounds. By selectively deprotecting the carbamate group under specific conditions, chemists can access the free amine functionality and further functionalize it to generate diverse chemical structures.Furthermore, the tert-butyl (3-aminocyclohexyl)carbamate is known for its stability and compatibility with a wide range of reaction conditions, making it a valuable tool for synthetic chemists working in the field of organic synthesis. Its versatility and reliability make it a valuable reagent for the construction of complex molecules with precise control over regioselectivity and stereoselectivity.